Data / Medical devices / United States / Biocircuit Technologies
Biocircuit Technologies: FDA-registered device maker in Atlanta, GA, United States, 3 510(k) clearances
Biocircuit Technologies is registered with the FDA (registration 3024511918) in Atlanta, GA, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated April 2, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3024511918
- Address
- 1819 Peachtree Rd Ne Ste 350, Atlanta, GA, United States, 30309
- Owner or operator
- BioCircuit Technologies (10086042)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- October 12, 2022
- Registered through
- 2026
- Brand names listed
- Nerve Tape
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cuff, Nerve | JXI | 2 | Complaint file establishment, Manufacturer, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 2, 2025 | K242113 | Nerve Wrap (07-DW-001-TAB) | JXI | Substantially Equivalent | Biocircuit Technologies, Inc. | accessdata.fda.gov |
| February 12, 2024 | K233533 | NerveTape | JXI | Substantially Equivalent | Biocircuit Technologies, Inc. | accessdata.fda.gov |
| July 15, 2022 | K210665 | Nerve Tape | JXI | Substantially Equivalent | Biocircuit Technologies, Incorporated | accessdata.fda.gov |
Compare with other makers
Updated April 2, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.